2-(Tributylstannyl)-1,3-oxazole

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Names

[ CAS No. ]:
145214-05-7

[ Name ]:
2-(Tributylstannyl)-1,3-oxazole

[Synonym ]:
tributylstannyloxazole
2-(Tri-n-butylstannyl)oxazole
2-(Tributylstannyl)-1,3-oxazole
2-tributylstannanyl-oxazole
2-(Tributylstannyl)oxazole
Oxazole,2-(tributylstannyl)
MFCD06798076
Oxazole, 2-(tributylstannyl)-
2-(tributylstannanyl)-1,3-oxazole
oxazole-2-SnBu3

Chemical & Physical Properties

[ Density]:
1.71 g/mL at 25ºC(lit.)

[ Boiling Point ]:
340.6±25.0 °C at 760 mmHg

[ Melting Point ]:
227-228℃

[ Molecular Formula ]:
C15H29NOSn

[ Molecular Weight ]:
358.107

[ Flash Point ]:
159.8±23.2 °C

[ Exact Mass ]:
359.127106

[ PSA ]:
26.03000

[ LogP ]:
8.61

[ Vapour Pressure ]:
0.0±0.7 mmHg at 25°C

[ Index of Refraction ]:
n20/D 1.4930(lit.)

[ Water Solubility ]:
Insoluble in water.

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS06, GHS08, GHS09

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H301-H312-H315-H319-H372-H410

[ Precautionary Statements ]:
Missing Phrase - N15.00950417-P260-P280-P305 + P351 + P338

[ Personal Protective Equipment ]:
Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
T: Toxic;N: Dangerous for the environment;

[ Risk Phrases ]:
R21

[ Safety Phrases ]:
S35

[ RIDADR ]:
UN 2788 6.1/PG 3

[ WGK Germany ]:
3

[ HS Code ]:
2934999090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • Oxazole
  • Chlorotributyltin

DownStream

  • Benzenamine, 4-methoxy-2-(2-oxazolyl)- (9CI)
  • Benzenamine, 4-ethoxy-2-(2-oxazolyl)- (9CI)
  • 2-(1,3-Oxazol-2-yl)aniline

Customs

[ HS Code ]: 2934999090

[ Summary ]:
2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

Synthesis of the eastern portion of ajudazol a based on Stille coupling and double acetylene carbocupration.

Org. Lett. 7 , 1063, (2005)

[structure: see text] A strategy for the synthesis of ajudazol A, an unusual, pharmacologically active metabolite from myxobacteria, based on the Stille cross-coupling of a 2-stannyl-oxazole with a vi...


More Articles

Related Compounds

  • 2-(Tributylstannyl)-1,3-thiazole
  • 2-(Tributylstannyl)-1,3-benzothiazole
  • (1Z,3E)-1,4-diphenyl-2-tributylstannyl-1,3-butadiene
  • (2R,4R)-4-phenyl-3-(benzenesulfonyl)-2-(tributylstannyl)-1,3-oxazolidine
  • tributyl-[1,3]dithian-2-yl-stannane
  • buta-1,3-dien-2-yl-tributylstannane
  • 1-(2-Methoxybenzenesulfonyl)-4-(1,2,5-thiadiazol-3-yl)piperazine
  • 1-(3,4-Difluorobenzenesulfonyl)-4-(1,2,5-thiadiazol-3-yl)piperazine
  • 1-(3-Chloro-2-methylbenzenesulfonyl)-4-(1,2,5-thiadiazol-3-yl)piperazine
  • 1-(3-Chloro-4-methoxybenzenesulfonyl)-4-(1,2,5-thiadiazol-3-yl)piperazine
  • 2-{[4-(1,2,5-Thiadiazol-3-yl)piperazin-1-yl]sulfonyl}benzonitrile
  • 1-[4-(1H-pyrazol-1-yl)benzenesulfonyl]-4-(1,2,5-thiadiazol-3-yl)piperazine
  • N-[1-(1,2,5-thiadiazol-3-yl)piperidin-4-yl]-2-(thiophen-2-yl)acetamide
  • 3,4-difluoro-N-[1-(1,2,5-thiadiazol-3-yl)piperidin-4-yl]benzamide
  • 2-(benzylsulfanyl)-N-[1-(1,2,5-thiadiazol-3-yl)piperidin-4-yl]acetamide
  • 2-[(4-fluorophenyl)sulfanyl]-N-[1-(1,2,5-thiadiazol-3-yl)piperidin-4-yl]acetamide
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